染色质
染色体构象捕获
荧光显微镜
荧光原位杂交
生物
原位
染色体
显微镜
计算生物学
基因组
基因组组织
原位杂交
DNA
细胞生物学
遗传学
荧光
基因
化学
基因表达
光学
物理
增强子
有机化学
作者
Pallas Kuo,Alice Darbyshire,Christophe Lambing
出处
期刊:Methods in molecular biology
日期:2022-01-01
卷期号:: 85-92
标识
DOI:10.1007/978-1-0716-2253-7_7
摘要
Chromatin organization influences gene and transposon expression, and regulates various cellular processes. Higher order chromatin structure has been widely studied using genomic approaches and microscopy image analyses. Chromosome conformation capture and sequencing the junction of DNA fragments enables the study of both chromatin interaction and chromosome folding. However, certain cell types are embedded in other cell types which complicate the process of studying them using high-throughput genomic approaches. To overcome this limitation, high-resolution microscopy techniques are now available to investigate chromatin organization in single cells. In this chapter, we provide a detailed protocol to prepare chromosome spreading from tomato nuclei, to label genomic loci by fluorescence in situ hybridization, and to visualize these locations at high resolution with Structured Illumination microscopy.
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